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Clinical Research Data Coordinator II
Emory UniversityData Coordinator II supporting the research program at Winship Cancer Institute. Responsible for data management, database operations, and facilitating study visits for clinical trials.
About the role
Key responsibilities & impact- Support the research program within the Clinical Trials Office (CTO) of Winship Cancer Institute (WCI)
- Responsible for facilitating initial visit with study subject
- Designs, builds, and maintains the functional operations of the database
- Increases the functionality of the database to meet internal customers' needs
- Manages complex projects related to data acquisition and tracking
- Analyzes subject data in relation to study protocol for entrance into study
- Ensures data from source is entered in EDC as per Sponsor contract expectations
- Facilitates study monitoring visits and prompt resolution of all study-related queries
Requirements
What you’ll need- Bachelor Degree and at least two (2) years of clinical research data management experience OR High School Diploma or GED and at least six (6) years of clinical research data management experience OR an equivalent combination of education and experience
- Certification/license: ACRP/SoCRA (or equivalent) certification preferred within three (3) years of hire.
Benefits
Comp & perks- Emory is an equal opportunity employer
- Participation in university programs
- Providing reasonable accommodations to qualified individuals with disabilities
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Data AcquisitionData TrackingEDC Data EntryStudy Protocol AnalysisFunctional Operations Management
Soft Skills
FacilitationProblem ResolutionCommunication
Certifications
ACRP CertificationSoCRA Certification